| #
|
String
|
Work count
|
String length
|
Publications with this string in their title
|
Sample work
|
Author name strings from such publications
|
| 1
|
species
|
128
|
7
|
π°
|
Adapt or disperse: understanding species persistence in a changing world
|
π
|
| 2
|
plant
geographical
|
87
10
|
5
12
|
π°
π°
|
Human food use increases plant geographical ranges in the Sonoran Desert
|
π
π
|
| 3
|
global
|
75
|
6
|
π°
|
Meta-analysis on the responses of traits of different taxonomic groups to global and local stressors
|
π
|
| 4
|
across
|
73
|
6
|
π°
|
From Reductionism to Reintegration: Solving society's most pressing problems requires building bridges between data types across the life sciences
|
π
|
| 5
|
diversity
using
richness
|
72
44
8
|
9
5
8
|
π°
π°
π°
|
How should we estimate diversity in the fossil record? Testing richness estimators using sampling-standardised discovery curves
|
π
π
π
|
| 6
|
functional
|
61
|
10
|
π°
|
A protocol for reproducible functional diversity analyses
|
π
|
| 7
|
ecological
towards
standard
|
57
21
8
|
10
7
8
|
π°
π°
π°
|
Towards an ecological traitβdata standard
|
π
π
π
|
| 8
|
conservation
|
54
|
12
|
π°
|
Threatened Species Initiative: Empowering conservation action using genomic resources
|
π
|
| 9
|
effects
assemblages
|
53
15
|
7
11
|
π°
π°
|
REMOVAL EXPERIMENT REVEALS LIMITED EFFECTS OF A BEHAVIORALLY DOMINANT SPECIES ON ANT ASSEMBLAGES
|
π
π
|
| 10
|
communities
changing
|
42
11
|
11
8
|
π°
π°
|
Diets maintained in a changing world: Does land-use intensification alter wild bee communities by selecting for flexible generalists?
|
π
π
|
| 11
|
forest
belowground
american
north
northern
|
42
12
11
10
|
6
11
8
5
|
π°
π°
π°
π°
π°
|
Aboveground impacts of a belowground invader: how invasive earthworms alter aboveground arthropod communities in a northern North American forest
|
π
π
π
π
π
|
| 12
|
variation
|
41
|
9
|
π°
|
Matrix projection models meet variation in the real world
|
π
|
| 13
|
plants
|
41
|
6
|
π°
|
Anagenetic evolution in island plants
|
π
|
| 14
|
patterns
ecology
world
predicting
|
40
36
18
9
|
8
7
5
10
|
π°
π°
π°
π°
|
Predicting patterns of stress and mortality in intertidal invertebrates: applications of biophysical ecology in a changing world
|
π
π
π
π
|
| 15
|
traits
impacts
recovery
|
39
14
8
|
6
7
8
|
π°
π°
π°
|
Animal population decline and recovery after severe fire: Relating ecological and life history traits with expert estimates of population impacts from the Australian 2019-20 megafires
|
π
π
π
|
| 16
|
between
their
competition
|
38
21
12
|
7
5
11
|
π°
π°
π°
|
Effects of an endogeic and an anecic earthworm on the competition between four annual plants and their relative fecundity
|
π
π
π
|
| 17
|
evolution
|
36
|
9
|
π°
|
Complexity of avian evolution revealed by family-level genomes
|
π
|
| 18
|
climate
|
36
|
7
|
π°
|
Masting is uncommon in trees that depend on mutualist dispersers in the context of global climate and fertility gradients
|
π
|
| 19
|
environmental
change
trends
scales
|
34
19
15
10
|
13
6
|
π°
π°
π°
π°
|
Three decades of environmental change studies at alpine Finse, Norway: climate trends and responses across ecological scales
|
π
π
π
π
|
| 20
|
ecosystem
|
32
|
9
|
π°
|
Rainfallβdependent impacts of threatened ecosystem engineers on organic matter cycling
|
π
|
| 21
|
scaling
|
32
|
7
|
π°
|
Modelling universality and scaling
|
π
|
| 22
|
model
|
32
|
5
|
π°
|
A dataβdriven semantic segmentation model for direct cardiac functional analysis based on undersampled radial MR cine series
|
π
|
| 23
|
evolutionary
history
|
31
16
|
12
7
|
π°
π°
|
EXOTICS EXHIBIT MORE EVOLUTIONARY HISTORY THAN NATIVES
|
π
π
|
| 24
|
australian
among
mortality
properties
|
31
24
9
8
|
10
5
9
|
π°
π°
π°
π°
|
Variation in fur properties may explain differences in heat-related mortality among Australian flying-foxes
|
π
π
π
π
|
| 25
|
models
|
30
|
6
|
π°
|
Tools for exploring mouse models of human disease
|
π
|
| 26
|
community
|
29
|
9
|
π°
|
A Common Yardstick to Measure the Effects of Different Extreme Climatic Events on Soil Arthropod Community Composition Using Time-Series Data
|
π
|
| 27
|
structure
avian
|
29
12
|
9
5
|
π°
π°
|
Source range phylogenetic community structure can predict the outcome of avian introductions
|
π
π
|
| 28
|
metabolic
|
28
|
9
|
π°
|
Comment on `A critical understanding of the fractal model of metabolic scaling'
|
π
|
| 29
|
research
|
28
|
8
|
π°
|
Standard methods for pollen research
|
π
|
| 30
|
tropical
under
|
28
12
|
8
5
|
π°
π°
|
Ground Spider Communities Under Tropical LandβUse Change
|
π
π
|
| 31
|
spatial
|
28
|
7
|
π°
|
Top-down response to spatial variation in productivity and bottom-up response to temporal variation in productivity in a long-term study of desert ants
|
π
|
| 32
|
growth
carbon
rates
efficiency
|
28
25
12
9
|
6
5
10
|
π°
π°
π°
π°
|
Role of carbon allocation efficiency in the temperature dependence of autotroph growth rates
|
π
π
π
π
|
| 33
|
population
|
27
|
10
|
π°
|
TetraDENSITY: A database of population density estimates in terrestrial vertebrates
|
π
|
| 34
|
approach
understanding
|
27
15
|
8
13
|
π°
π°
|
A hierarchical approach to understanding physiological associations with climate
|
π
π
|
| 35
|
thermal
review
|
27
10
|
7
6
|
π°
π°
|
Half a century of thermal tolerance studies in springtails (Collembola): A review of metrics, spatial and temporal trends
|
π
π
|
| 36
|
responses
|
26
|
9
|
π°
|
Nitrogen productivity and allocation responses of 12 important tree species to increased CO2
|
π
|
| 37
|
response
|
26
|
8
|
π°
|
Detection of the metabolic response to drought stress using hyperspectral reflectance
|
π
|
| 38
|
analysis
testing
knowledge
differences
|
26
16
11
10
|
8
7
9
11
|
π°
π°
π°
π°
|
Differences in STI knowledge accuracy and STI/HIV testing among a random sample of college students: A secondary survey analysis
|
π
π
π
π
|
| 39
|
dynamics
shifts
|
26
10
|
8
6
|
π°
π°
|
Rapid poleward distributional shifts in the European cave-dwelling Meta spiders under the influence of competition dynamics
|
π
π
|
| 40
|
study
relationships
|
26
16
|
5
13
|
π°
π°
|
Study of soilβvegetation relationships on the Butte Montceau in Fontainebleau, France: Pedagogical exercise and training report
|
π
π
|
| 41
|
different
|
25
|
9
|
π°
|
Ecology: How different are Australian ecosystems and ecologists?
|
π
|
| 42
|
human
threatened
|
24
9
|
5
10
|
π°
π°
|
Half of the worldβs tree biodiversity is unprotected and is increasingly threatened by human activities
|
π
π
|
| 43
|
temperature
|
23
|
11
|
π°
|
Global maps of soil temperature
|
π
|
| 44
|
nitrogen
|
23
|
8
|
π°
|
Soil carbon and nitrogen cycling and storage throughout the soil profile in a sweetgum plantation after 11 years of CO2-enrichment
|
π
|
| 45
|
terrestrial
|
22
|
11
|
π°
|
The island rule explains consistent patterns of body size evolution in terrestrial vertebrates
|
π
|
| 46
|
composition
|
22
|
11
|
π°
|
Wild bee larval food composition in five European cities
|
π
|
| 47
|
ecosystems
genomic
novel
|
22
10
9
|
10
7
5
|
π°
π°
π°
|
Novel integrative elements and genomic plasticity in ocean ecosystems
|
π
π
π
|
| 48
|
monitoring
|
21
|
10
|
π°
|
Modern Approaches to the Monitoring of BiΠΎdiversity (MAMBO)
|
π
|
| 49
|
changes
associated
|
21
10
|
7
10
|
π°
π°
|
Importance of local changes in leaf height and density to fish and decapods associated with seagrasses
|
π
π
|
| 50
|
network
protected
|
21
18
|
7
9
|
π°
π°
|
Connectivity of the global network of protected areas
|
π
π
|
| 51
|
distribution
|
20
|
12
|
π°
|
A predominantly southern distribution conceals a northern reservoir of diversity in a wet sclerophyll tree
|
π
|
| 52
|
abundance
insect
|
20
13
|
9
6
|
π°
π°
|
Asynchrony in terrestrial insect abundance corresponds with species traits
|
π
π
|
| 53
|
insects
|
20
|
7
|
π°
|
Editorial overview: Behavioural ecology of insects and its metamorphosis into a multidisciplinary field
|
π
|
| 54
|
trait
|
20
|
5
|
π°
|
Interspecific integration of trait dimensions at local scales: the plant phenotype as an integrated network
|
π
|
| 55
|
biological
|
19
|
10
|
π°
|
Fifty years of the Biological Records Centre
|
π
|
| 56
|
hypothesis
|
19
|
10
|
π°
|
Convergent evolutionary patterns of heterostyly across angiosperms support the pollination-precision hypothesis
|
π
|
| 57
|
multiple
|
19
|
8
|
π°
|
Selection for associative learning of color stimuli reveals correlated evolution of this learning ability across multiple stimuli and rewards
|
π
|
| 58
|
effect
|
19
|
6
|
π°
|
Testing the novelty effect of an m-learning tool on internalization and achievement: A Self-Determination Theory approach
|
π
|
| 59
|
water
areas
importance
|
19
14
10
|
5
10
|
π°
π°
π°
|
Areas of global importance for terrestrial biodiversity, carbon, and water
|
π
π
π
|
| 60
|
field
relationship
pesticides
|
19
11
10
|
5
12
10
|
π°
π°
π°
|
Relationship between agricultural pesticides and the diet of riparian spiders in the field
|
π
π
π
|
| 61
|
phylogenetic
|
18
|
12
|
π°
|
Both sourceβ and recipientβrange phylogenetic community structure can predict the outcome of avian introductions
|
π
|
| 62
|
populations
assessing
|
18
14
|
11
9
|
π°
π°
|
Recommendations for assessing earthworm populations in Brazilian ecosystems
|
π
π
|
| 63
|
framework
|
18
|
9
|
π°
|
Developing a scalable framework for partnerships between health agencies and the Wikimedia ecosystem
|
π
|
| 64
|
database
spiders
|
18
12
|
8
7
|
π°
π°
|
A trait database and updated checklist for European subterranean spiders
|
π
π
|
| 65
|
evidence
|
18
|
8
|
π°
|
Non-vascular plants as a food source for litter-dwelling Collembola: Field evidence
|
π
|
| 66
|
warming
long-term
collembola
|
18
12
10
|
7
9
10
|
π°
π°
π°
|
Functional diversity of Collembola is reduced in soils subjected to short-term, but not long-term, geothermal warming
|
π
π
π
|
| 67
|
niche
|
18
|
5
|
π°
|
Multidimensional trophic niche revealed by complementary approaches: gut content, digestive enzymes, fatty acids and stable isotopes in soil fauna
|
π
|
| 68
|
distributions
studies
|
17
8
|
13
7
|
π°
π°
|
Efficient Permutation-based Genome-wide Association Studies for Normal and Skewed Phenotypic Distributions
|
π
π
|
| 69
|
interactions
|
17
|
12
|
π°
|
Intraspecific variation in species interactions promotes the feasibility of mutualistic assemblages
|
π
|
| 70
|
vegetation
urban
|
17
10
|
10
5
|
π°
π°
|
Severe vegetation degradation associated with different disturbance types in a poorly managed urban recreation destination in Iran
|
π
π
|
| 71
|
evaluation
|
17
|
10
|
π°
|
Shortfalls in Conservation Evidence: Moving from Ecological Effects of Interventions to Policy Evaluation
|
π
|
| 72
|
networks
|
17
|
8
|
π°
|
Species-habitat networks: Bridging applied ecology and network theory
|
π
|
| 73
|
drivers
local
|
17
13
|
7
5
|
π°
π°
|
Global environmental drivers of local abundance-mass scaling in soil animal communities
|
π
π
|
| 74
|
limits
performance
birds
|
17
15
11
|
6
11
5
|
π°
π°
π°
|
Performance of a points-based scoring system for assessing species limits in birds
|
π
π
π
|
| 75
|
shape
|
17
|
5
|
π°
|
Author Correction: Symbioses shape feeding niches and diversification across insects
|
π
|
| 76
|
experimental
|
16
|
12
|
π°
|
Trophic transfer of polyunsaturated fatty acids across the aquaticβterrestrial interface: An experimental tritrophic food chain approach
|
π
|
| 77
|
management
|
16
|
10
|
π°
|
iKNOW- A Knowledge Graph Management Platform for the Biodiversity Domain
|
π
|
| 78
|
forests
|
16
|
7
|
π°
|
Functional diversity underlies demographic responses to environmental variation in European forests
|
π
|
| 79
|
marine
mammals
|
16
14
|
6
7
|
π°
π°
|
Survival improvements of marine mammals in zoological institutions mirror historical advances in human longevity
|
π
π
|
| 80
|
demographic
|
15
|
11
|
π°
|
Demographic performance of European tree species at their hot and cold climatic edges
|
π
|
| 81
|
integrating
|
15
|
11
|
π°
|
Towards integrating and harmonising information on plant invasions across Australia
|
π
|
| 82
|
during
variability
climatic
|
15
13
12
|
6
11
8
|
π°
π°
π°
|
High-resolution quantification of earthworm calcite granules from western European loess sequences reveals stadial-interstadial climatic variability during the Last Glacial
|
π
π
π
|
| 83
|
theory
|
15
|
6
|
π°
|
The effects of m-learning on motivation, achievement and well-being: A Self-Determination Theory approach
|
π
|
| 84
|
coral
integrated
|
15
8
|
5
10
|
π°
π°
|
What's left in the tank? Identification of non-ascribed aquarium's coral collections with DNA barcodes as part of an integrated diagnostic approach
|
π
π
|
| 85
|
diversification
morphological
|
14
9
|
15
13
|
π°
π°
|
Profile of a flower: How rates of morphological evolution drive floral diversification in Ericales and angiosperms
|
π
π
|
| 86
|
implications
|
14
|
12
|
π°
|
Cross-species patterns in the coordination between leaf and stem traits, and their implications for plant hydraulics
|
π
|
| 87
|
development
|
14
|
11
|
π°
|
Plant homeostasis, growth and development in natural and artificial soils
|
π
|
| 88
|
strategies
|
14
|
10
|
π°
|
Shifts in plant functional strategies over the course of wheat domestication
|
π
|
| 89
|
microbial
|
14
|
9
|
π°
|
Microbial Community Structure in a Malaysian Tropical Peat Swamp Forest: The Influence of Tree Species and Depth
|
π
|
| 90
|
function
woody
|
14
|
8
5
|
π°
π°
|
Cross-species relationships between seedling relative growth rate, nitrogen productivity and root vs leaf function in 28 Australian woody species
|
π
π
|
| 91
|
costs
phenotypic
adaptation
|
14
8
|
5
10
|
π°
π°
π°
|
The costs of phenotypic adaptation to repeatedly fluctuating temperatures in a soil arthropod
|
π
π
π
|
| 92
|
space
major
|
14
9
|
5
|
π°
π°
|
A widespread thermodynamic effect, but maintenance of biological rates through space across life's major domains
|
π
π
|
| 93
|
three
|
14
|
5
|
π°
|
Taste for pollen comes in different shapes: Consumption by tadpoles from three divergent ecomorphotypes
|
π
|
| 94
|
along
|
14
|
5
|
π°
|
Assessing trait driver theory along abiotic gradients in tropical plant communities
|
π
|
| 95
|
availability
landscape
|
13
12
|
12
9
|
π°
π°
|
Interaction between warming and landscape foraging resource availability on solitary bee reproduction
|
π
π
|
| 96
|
antarctic
conserving
|
13
10
|
9
10
|
π°
π°
|
Threat management priorities for conserving Antarctic biodiversity
|
π
π
|
| 97
|
tolerance
|
13
|
9
|
π°
|
Brain size predicts bees' tolerance to urban environments
|
π
|
| 98
|
modelling
|
13
|
9
|
π°
|
Advances in Monitoring and Modelling Climate at Ecologically Relevant Scales
|
π
|
| 99
|
european
|
13
|
8
|
π°
|
National records of 3000 European bee and hoverfly species: A contribution to pollinator conservation
|
π
|
| 100
|
habitat
|
13
|
7
|
π°
|
Synergistic effects of habitat fragmentation and hunting on the extinction risk of neotropical primates
|
π
|
| 101
|
through
integration
|
13
9
|
7
11
|
π°
π°
|
Alleviating Environmental Health Disparities Through Community Science and Data Integration
|
π
π
|
| 102
|
method
common
|
13
|
6
|
π°
π°
|
Leaf-size divergence along rainfall and soil-nutrient gradients: is the method of size reduction common among clades?
|
π
π
|
| 103
|
island
sub-antarctic
invertebrate
|
13
9
8
|
6
13
12
|
π°
π°
π°
|
Morphometric measurement selection: an invertebrate case study based on weevils from sub-Antarctic Marion Island
|
π
π
π
|
| 104
|
animal
|
13
|
6
|
π°
|
Global monitoring of soil animal communities using a common methodology
|
π
|
| 105
|
trees
|
13
|
5
|
π°
|
The role of functional uniqueness and spatial aggregation in explaining rarity in trees
|
π
|
| 106
|
biodiversity
|
12
|
12
|
π°
|
Predictions of biodiversity are improved by integrating trait-based competition with abiotic filtering
|
π
|
| 107
|
perspective
|
12
|
11
|
π°
|
Hematological parameters of a Neotropical wild frog population, with a phylogenetic perspective on blood cell composition in Anura
|
π
|
| 108
|
challenges
|
12
|
10
|
π°
|
Building a Global Ecosystem Research Infrastructure to Address Global Grand Challenges for Macrosystem Ecology
|
π
|
| 109
|
allocation
|
12
|
10
|
π°
|
Comparing resource exploitation and allocation of two closely related aphid parasitoids sharing the same host
|
π
|
| 110
|
synthesis
|
12
|
9
|
π°
|
Data Proliferation, Reconciliation, and Synthesis in Viral Ecology
|
π
|
| 111
|
potential
|
12
|
9
|
π°
|
Assessing the conservation potential of fish and corals in aquariums globally
|
π
|
| 112
|
modeling
|
12
|
8
|
π°
|
Long-term leaf C:N ratio change under elevated CO2 and nitrogen deposition in China: Evidence from observations and process-based modeling
|
π
|
| 113
|
surface
|
12
|
7
|
π°
|
Updated respiration routines alter spatio-temporal patterns of carbon cycling in a global land surface model
|
π
|
| 114
|
general
|
12
|
7
|
π°
|
For fluxβs sake: General considerations for energy-flux calculations in ecological communities
|
π
|
| 115
|
future
|
12
|
6
|
π°
|
The commonness of rarity: Global and future distribution of rarity across land plants
|
π
|
| 116
|
alpine
|
12
|
6
|
π°
|
Variation in Ξ΄13C and Ξ΄15N within and among plant species in the alpine tundra
|
π
|
| 117
|
reply
|
12
|
5
|
π°
|
Pawar et al. reply
|
π
|
| 118
|
temperatures
|
11
|
12
|
π°
|
Insects at low temperatures: an ecological perspective
|
π
|
| 119
|
reproductive
|
11
|
12
|
π°
|
Pollinator asynchrony drives the temporal stability of flower visitation rates, but not of plant reproductive success
|
π
|
| 120
|
subterranean
|
11
|
12
|
π°
|
Towards evidenceβbased conservation of subterranean ecosystems
|
π
|
| 121
|
approaches
|
11
|
10
|
π°
|
Bootstrapping outperforms communityβweighted approaches for estimating the shapes of phenotypic distributions
|
π
|
| 122
|
morphology
|
11
|
10
|
π°
|
Morphology and burrowing energetics of semi-fossorial skinks (Liopholis spp.).
|
π
|
| 123
|
extinction
|
11
|
10
|
π°
|
On the timing of megafaunal extinction and associated floristic consequences in Australia through the lens of functional palaeoecology
|
π
|
| 124
|
assessment
|
11
|
10
|
π°
|
Developing a standardized definition of ecosystem collapse for risk assessment
|
π
|
| 125
|
taxonomic
|
11
|
9
|
π°
|
On four measures of taxonomic richness
|
π
|
| 126
|
sampling
|
11
|
8
|
π°
|
Corrigendum to "Calibration and field application of passive sampling for episodic exposure to polar organic pesticides in streams" [Environ. Pollut. 194 (2014) 196-202]
|
π
|
| 127
|
exchange
leaves
|
11
9
|
8
6
|
π°
π°
|
Biotic exchange leaves detectable genomic patterns in the Australian rain forest flora
|
π
π
|
| 128
|
turnover
|
11
|
8
|
π°
|
Miocene biome turnover drove conservative body size evolution across Australian vertebrates
|
π
|
| 129
|
science
policy
|
11
8
|
7
6
|
π°
π°
|
Sustainability Agenda for the Pantanal Wetland: Perspectives on a Collaborative Interface for Science, Policy, and Decision-Making
|
π
π
|
| 130
|
system
|
11
|
6
|
π°
|
EVOLUTION IN A LABORATORY HOSTβPARASITOID SYSTEM AND ITS EFFECT ON POPULATION KINETICS
|
π
|
| 131
|
stress
|
11
|
6
|
π°
|
Temperature-induced plasticity in egg size and resistance of eggs to temperature stress in a soil arthropod
|
π
|
| 132
|
range
|
11
|
5
|
π°
|
Leaf mesophyll diffusion conductance in 35 Australian sclerophylls covering a broad range of foliage structural and physiological variation
|
π
|
| 133
|
south
australia
years
|
11
10
9
|
5
9
|
π°
π°
π°
|
Grasshopper country before and after: a resurvey of Ken Key's collecting expeditions in New South Wales, Australia, 70 years on
|
π
π
π
|
| 134
|
constraints
|
10
|
11
|
π°
|
Life-history strategies as a tool to identify conservation constraints: A case-study on ants in chalk grasslands
|
π
|
| 135
|
application
|
10
|
11
|
π°
|
A modern pollen-climate calibration set from central-western Mongolia and its application to a late glacial-Holocene record
|
π
|
| 136
|
angiosperm
|
10
|
10
|
π°
|
The maleness of larger angiosperm flowers
|
π
|
| 137
|
estimating
quality
|
10
9
|
10
7
|
π°
π°
|
Aboveground litter quality is a better predictor than belowground microbial communities when estimating carbon mineralization along a land-use gradient
|
π
π
|
| 138
|
gradients
|
10
|
9
|
π°
|
Changes amid constancy: flower and leaf microbiomes along land use gradients and between bioregions
|
π
|
| 139
|
resources
ontology
|
10
|
9
8
|
π°
π°
|
Data sharing and ontology use among agricultural genetics, genomics, and breeding databases and resources of the Agbiodata Consortium
|
π
π
|
| 140
|
disease
temporal
|
10
9
|
7
8
|
π°
π°
|
Climate predicts geographic and temporal variation in mosquito-borne disease dynamics on two continents
|
π
π
|
| 141
|
within
|
10
|
6
|
π°
|
An integrative re-evaluation of Typhlatya shrimp within the karst aquifer of the YucatΓ‘n Peninsula, Mexico
|
π
|
| 142
|
groups
|
10
|
6
|
π°
|
How good are epigeic earthworms at dispersing? An investigation to compare epigeic to endogeic and anecic groups
|
π
|
| 143
|
environments
|
9
|
12
|
π°
|
Sapwood capacitance is greater in evergreen sclerophyll species growing in high compared to low-rainfall environments
|
π
|
| 144
|
applications
|
9
|
12
|
π°
|
Exploring Ensemble Applications for Multi-sequence Myocardial Pathology Segmentation
|
π
|
| 145
|
acclimation
|
9
|
11
|
π°
|
Testing the beneficial acclimation hypothesis and its alternatives for locomotor performance
|
π
|
| 146
|
environment
|
9
|
11
|
π°
|
Rohingya refugees and the environment
|
π
|
| 147
|
physiology
|
9
|
10
|
π°
|
Investigating onychophoran gas exchange and water balance as a means to inform current controversies in arthropod physiology
|
π
|
| 148
|
complexity
|
9
|
10
|
π°
|
Dealing with software complexity in individualβbased models
|
π
|
| 149
|
butterfly
|
9
|
9
|
π°
|
Synchrony of butterfly populations across species' geographic ranges
|
π
|
| 150
|
phenotype
|
9
|
9
|
π°
|
Characterizing Long COVID: Deep Phenotype of a Complex Condition
|
π
|
| 151
|
assembly
|
9
|
8
|
π°
|
A systematic comparison of chloroplast genome assembly tools
|
π
|
| 152
|
diseases
|
9
|
8
|
π°
|
The Monarch Initiative in 2024: an analytic platform integrating phenotypes, genes and diseases across species
|
π
|
| 153
|
exposure
|
9
|
8
|
π°
|
Rapid shift in thermal resistance between generations through maternal heat exposure
|
π
|
| 154
|
bacteria
|
9
|
8
|
π°
|
Putative roles of bacteria in the carbon and nitrogen cycles in a tropical peat swamp forest
|
π
|
| 155
|
systems
|
9
|
7
|
π°
|
CSR ecological strategies and plant mating systems: outcrossing increases with competitiveness but stress-tolerance is related to mixed mating
|
π
|
| 156
|
genetic
|
9
|
7
|
π°
|
An earlier formulation of the genetic conflict hypothesis of genomic imprinting
|
π
|
| 157
|
biology
|
9
|
7
|
π°
|
Germination biology of selected central Australian plants
|
π
|
| 158
|
energy
|
9
|
6
|
π°
|
Combining heat-transfer and energy budget models to predict thermal stress in Mediterranean intertidal mussels
|
π
|
| 159
|
drive
|
9
|
5
|
π°
|
Feedback loops drive ecological succession: towards a unified conceptual framework
|
π
|
| 160
|
opportunities
foraging
|
8
|
13
8
|
π°
π°
|
Modelling the joint effects of body size and microclimate on heat budgets and foraging opportunities of ectotherms
|
π
π
|
| 161
|
productivity
|
8
|
12
|
π°
|
Neighbor Diversity Regulates the Productivity of Coral Assemblages
|
π
|
| 162
|
priorities
|
8
|
10
|
π°
|
Aligning marine spatial conservation priorities with functional connectivity across maritime jurisdictions
|
π
|
| 163
|
plasticity
|
8
|
10
|
π°
|
Indigenous and introduced Collembola differ in desiccation resistance but not its plasticity in response to temperature
|
π
|
| 164
|
endangered
|
8
|
10
|
π°
|
Plant-arthropod interactions of an endangered California lupine
|
π
|
| 165
|
production
|
8
|
10
|
π°
|
Modelling approach to analyse the effects of nitrification inhibition on primary production
|
π
|
| 166
|
national
|
8
|
8
|
π°
|
Developing a national indicator of functional connectivity
|
π
|
| 167
|
gradient
|
8
|
8
|
π°
|
Molluscs along a salinity gradient in a hypersaline coastal lagoon, southern Gulf of Mexico
|
π
|
| 168
|
resource
|
8
|
8
|
π°
|
Endangered species recovery: A resource allocation problem
|
π
|
| 169
|
trophic
|
8
|
7
|
π°
|
Trophic consistency of supraspecific taxa in belowground invertebrate communities
|
π
|
| 170
|
aquatic
|
8
|
7
|
π°
|
Impact of warming on aquatic body sizes explained by metabolic scaling from microbes to macrofauna
|
π
|
